Verifying…
Home / Drug A–Z / Eden Propranolol Hydrochloride 40 mg

Eden Propranolol Hydrochloride 40 mg

NAFDAC Reg. No. B4-9819 · Drug

Registered with NAFDAC. Registration activeAs of 27 October 2026 · synced automatically from official sources.
Product
Eden Propranolol Hydrochloride 40 mg
NAFDAC number
B4-9819
Active ingredient
Propranolol Hydrochloride
Strength
40 mg
Form
Tablet
Pack size
5 x 10's (in PVC-Alu blisters)
Manufacturer
Not listed
Applicant (holder)
Eden U-K Pharm Ltd
Approved
28 Aug 2024
Status
Active View on NAFDAC ↗
Registration valid to
27 Aug 2029
WHO alerts
None found
Community reports
None
Times checked
0

What we found

  • Eden Propranolol Hydrochloride 40 mg is on the NAFDAC register with an active registration (B4-9819). A valid number alone does not prove a pack is genuine — counterfeiters copy real numbers, so also check the expiry date, seal and print quality.

Generated automatically from the NAFDAC register, WHO alerts and community data as of today. This is not medical advice. Always follow your doctor or pharmacist.

What Eden Propranolol Hydrochloride 40 mg is used for

From the official U.S. FDA label for propranolol hydrochloride, the active ingredient registered with NAFDAC.

What it is used for

Cardiac Arrhythmias Intravenous administration is usually reserved for life-threatening arrhythmias or those occurring under anesthesia. 1. Supraventricular arrhythmias Intravenous propranolol is indicated for the short-term treatment of supraventricular tachycardia, including Wolff-Parkinson-White syndrome and thyrotoxicosis, to decrease ventricular rate. Use in patients with atrial flutter or atrial fibrillation should be reserved for arrythmias unresponsive to standard therapy or when more prolonged control is required. Reversion to normal sinus rhythm has occasionally been observed, predominantly in patients with sinus or atrial tachycardia. 2. …

Possible side effects

To report SUSPECTED ADVERSE REACTIONS, contact Fresenius Kabi USA, LLC at 1-800-551-7176 or FDA at 1-800-FDA-1088 or www.fda.gov/medwatch. In a series of 225 patients, there were 6 deaths (see CLINICAL STUDIES). Cardiovascular events (hypotension, congestive heart failure, bradycardia, and heart block) were the most common. The only other event reported by more than one patient was nausea. Other adverse events for intravenous propranolol, reported during postmarketing surveillance include cardiac arrest, dyspnea, and cutaneous ulcers. …

Do not use if

Propranolol is contraindicated in 1) cardiogenic shock, 2) sinus bradycardia and greater than first-degree block, 3) bronchial asthma, 4) in patients with known hypersensitivity to propranolol.

Warnings

Cardiac Failure Sympathetic stimulation may be a vital component supporting circulatory function in patients with congestive heart failure, and its inhibition by beta-blockade may precipitate more severe failure. Although beta-blockers should be avoided in overt congestive heart failure, some have been shown to be highly beneficial when used with close follow-up in patients with a history of failure who are well compensated and are receiving additional therapies, including diuretics as needed. Beta-adrenergic blocking agents do not abolish the inotropic action of digitalis on heart muscle. …

General information only, not dosing advice. Always follow the leaflet in your pack and your doctor or pharmacist.

Check your pack of Eden Propranolol Hydrochloride 40 mg

Add the expiry date on your pack for a full Trust Score.

3 free checks left today Official sources: NAFDAC Green Book & recalls · WHO · U.S. FDA · NLM RxNorm

About Eden Propranolol Hydrochloride 40 mg

What is in Eden Propranolol Hydrochloride 40 mg?

Eden Propranolol Hydrochloride 40 mg contains Propranolol Hydrochloride (40 mg), as tablet, according to its NAFDAC registration record.

Is Eden Propranolol Hydrochloride 40 mg registered with NAFDAC?

Yes. Eden Propranolol Hydrochloride 40 mg is listed on the NAFDAC register under registration number B4-9819, and its registration is active as of 27 October 2026.

Has Eden Propranolol Hydrochloride 40 mg been flagged as fake or recalled?

No WHO falsified or substandard medical product alert currently matches Eden Propranolol Hydrochloride 40 mg in our automatically synced alert list.

How can I check that my pack of Eden Propranolol Hydrochloride 40 mg is genuine?

Run a free authenticity scan with the NAFDAC number B4-9819, your pack's expiry date and batch number to get a Trust Score, compare the pack with the NAFDAC record (ingredient, strength, form, manufacturer), and buy only from licensed pharmacies.

What is Eden Propranolol Hydrochloride 40 mg used for?

Cardiac Arrhythmias Intravenous administration is usually reserved for life-threatening arrhythmias or those occurring under anesthesia. 1. Supraventricular arrhythmias Intravenous propranolol is indicated for the short-term treatment of supraventricular tachycardia, including Wolff-Parkinson-White syndrome and thyrotoxicosis, to decrease ventricular rate. Use in patients with atrial flutter or at (Summarised from the official U.S. FDA label for propranolol hydrochloride. Always follow your doctor or pharmacist.)

Patient reviews

–No reviews yet
5★
0
4★
0
3★
0
2★
0
1★
0
Have you used Eden Propranolol Hydrochloride 40 mg? Share your experience to help other patients. Sign in to review

Reviews are personal experiences from PillVera users, not medical advice. Report side effects to your doctor and to NAFDAC.